Canonical Allele Identifier: PA2825752871
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 471308
ClinVar RCV Id: RCV000552425 RCV000595695 RCV001274843 RCV001507565 RCV003960357
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124450.1:p.Val1525Ile
CA1707094
NM_001130978.2:c.4573G>A